FARS2 Polyclonal Antibody

Background:
This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants.

Synonyms:
FARS2, COXPD14, FARS1, HSPC320, PheRS, SPG77

Immunogen: Recombinant fusion protein of human FARS2 (NP_006558.1).

Swissprot: O95363
Gene ID: 10667

Calculated MW: 52 kDa
Observed MW: 52 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000"

Storage:
Store at -20°C. Avoid freeze / thaw cycles.